Presumed spinocerebellar ataxia 7: challenges without molecular diagnosis
Clin Exp Optom
.
2021 May;104(4):547-549.
doi: 10.1080/08164622.2021.1878822.
Epub 2021 Feb 25.
Authors
He Li
1
,
Fatoumata Yanoga
1
,
Mohamed H Abdel-Rahman
1
2
,
Colleen M Cebulla
1
Affiliations
1
Havener Eye Institute, Department of Ophthalmology and Visual Science, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
2
Division of Human Genetics, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
PMID:
33689625
DOI:
10.1080/08164622.2021.1878822
No abstract available
Keywords:
Inherited retinal degeneration; spinocerebellar ataxia 7.
MeSH terms
Humans
Spinocerebellar Ataxias* / diagnosis
Spinocerebellar Ataxias* / genetics